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Daniel H Geschwind

Showing results (221-230 of 474) with videos related to

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Iscience|February 22, 2021
Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factorsTimothy S Chang, Yi Ding, Malika K Freund, et al.
Science Translational Medicine|January 23, 2015
Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autismOlga Peñagarikano, María T Lázaro, Xiao-Hong Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Science (New York, N.Y.)|August 18, 2022
Functional regulatory variants implicate distinct transcriptional networks in dementiaYonatan A Cooper, Noam Teyssier, Nina M Dräger, et al.
Nucleic Acids Research|March 14, 2015
Genome engineering of isogenic human ES cells to model autism disordersRefugio A Martinez, Jason L Stein, Anne-Rachel F Krostag, et al.
Annals of Neurology|December 14, 2011
A gene expression phenotype in lymphocytes from Friedreich ataxia patientsGiovanni Coppola, Ryan Burnett, Susan Perlman, et al.
Nature Neuroscience|February 23, 2021
Long-term maturation of human cortical organoids matches key early postnatal transitionsAaron Gordon, Se-Jin Yoon, Stephen S Tran, et al.
Dementia and Geriatric Cognitive Disorders|September 29, 2011
Cortical and hippocampal atrophy in patients with autosomal dominant familial Alzheimer's diseaseLiana G Apostolova, Kristy S Hwang, Luis D Medina, et al.
Journal of Neurosurgery. Pediatrics|October 27, 2023
Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosisEmre Kiziltug, Phan Q Duy, Garrett Allington, et al.
Human Molecular Genetics|June 21, 2019
Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissueChloe C Y Wong, Rebecca G Smith, Eilis Hannon, et al.
Pageof 48

Showing results (221-230 of 474) with videos related to

Sort By:
Pageof 48
Iscience|February 22, 2021
Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factorsTimothy S Chang, Yi Ding, Malika K Freund, et al.
Science Translational Medicine|January 23, 2015
Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autismOlga Peñagarikano, María T Lázaro, Xiao-Hong Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 28, 2023
The contributions of rare inherited and polygenic risk to ASD in multiplex familiesMatilde Cirnigliaro, Timothy S Chang, Stephanie A Arteaga, et al.
Science (New York, N.Y.)|August 18, 2022
Functional regulatory variants implicate distinct transcriptional networks in dementiaYonatan A Cooper, Noam Teyssier, Nina M Dräger, et al.
Nucleic Acids Research|March 14, 2015
Genome engineering of isogenic human ES cells to model autism disordersRefugio A Martinez, Jason L Stein, Anne-Rachel F Krostag, et al.
Annals of Neurology|December 14, 2011
A gene expression phenotype in lymphocytes from Friedreich ataxia patientsGiovanni Coppola, Ryan Burnett, Susan Perlman, et al.
Nature Neuroscience|February 23, 2021
Long-term maturation of human cortical organoids matches key early postnatal transitionsAaron Gordon, Se-Jin Yoon, Stephen S Tran, et al.
Dementia and Geriatric Cognitive Disorders|September 29, 2011
Cortical and hippocampal atrophy in patients with autosomal dominant familial Alzheimer's diseaseLiana G Apostolova, Kristy S Hwang, Luis D Medina, et al.
Journal of Neurosurgery. Pediatrics|October 27, 2023
Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosisEmre Kiziltug, Phan Q Duy, Garrett Allington, et al.
Human Molecular Genetics|June 21, 2019
Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissueChloe C Y Wong, Rebecca G Smith, Eilis Hannon, et al.
Pageof 48